TY - JOUR
T1 - Distribution and functional significance of rodent cerebellar glycogen
AU - Akther, Sonam
AU - Lee, Ashley Bomin
AU - Konno, Ayumu
AU - Asiminas, Antonis
AU - Vittani, Marta
AU - Mishima, Tsuneko
AU - Hirai, Hirokazu
AU - Meehan, Claire Francesca
AU - Duran, Jordi
AU - Guinovart, Joan
AU - Ashida, Hitoshi
AU - Morita, Tsuyoshi
AU - Baba, Otto
AU - Shigemoto, Ryuichi
AU - Nedergaard, Maiken
AU - Hirase, Hajime
N1 - Publisher Copyright:
© 2026 The Author(s)
PY - 2026/4/17
Y1 - 2026/4/17
N2 - The mammalian brain stores glucose, the main circulating energy substrate, as glycogen. In rodents, the cerebellum contains relatively high glycogen levels, yet its cellular and subcellular distribution remains poorly defined. Using monoclonal antibodies against glycogen, we examined its distribution in the mouse cerebellar cortex. Glycogen was predominantly localized to Bergmann glia (BG) processes in the molecular layer and was also detected in Purkinje cells (PCs), the principal cerebellar neurons. To assess the functional significance of cerebellar glycogen, we analyzed behavior in mice lacking glycogen synthase 1 (Gys1) in BG or PCs using a floxed Gys1 line. Gys1 deficiency in either PCs or GFAP-positive cells reduced anxiety-like behavior, whereas combined deletion caused PC degeneration and ataxia. These findings reveal a critical role for glycogen metabolism in both astrocytes and neurons in cerebellar function.
AB - The mammalian brain stores glucose, the main circulating energy substrate, as glycogen. In rodents, the cerebellum contains relatively high glycogen levels, yet its cellular and subcellular distribution remains poorly defined. Using monoclonal antibodies against glycogen, we examined its distribution in the mouse cerebellar cortex. Glycogen was predominantly localized to Bergmann glia (BG) processes in the molecular layer and was also detected in Purkinje cells (PCs), the principal cerebellar neurons. To assess the functional significance of cerebellar glycogen, we analyzed behavior in mice lacking glycogen synthase 1 (Gys1) in BG or PCs using a floxed Gys1 line. Gys1 deficiency in either PCs or GFAP-positive cells reduced anxiety-like behavior, whereas combined deletion caused PC degeneration and ataxia. These findings reveal a critical role for glycogen metabolism in both astrocytes and neurons in cerebellar function.
KW - Cellular neuroscience
KW - Molecular neuroscience
UR - https://www.scopus.com/pages/publications/105032875953
UR - http://hdl.handle.net/20.500.14342/6196
U2 - 10.1016/j.isci.2026.115192
DO - 10.1016/j.isci.2026.115192
M3 - Article
AN - SCOPUS:105032875953
SN - 2589-0042
VL - 29
JO - iScience
JF - iScience
IS - 4
M1 - 115192
ER -